posted on 2022-10-27, 04:16authored byTomasz Urbaniak, Gabriela S. García-Briones, Alexander Zhigunov, Sviatoslav Hladysh, Edyta Adrian, Volodymyr Lobaz, Tereza Krunclová, Olga Janoušková, Ognen Pop-Georgievski, Dana Kubies
Layer-by-layer (LbL)
polyelectrolyte coatings are intensively studied
as reservoirs of bioactive proteins for modulating interactions between
biomaterial surfaces and cells. Mild conditions for the incorporation
of growth factors into delivery systems are required to maintain protein
bioactivity. Here, we present LbL films composed of water-soluble N-[(2-hydroxy-3-trimethylammonium)propyl] chitosan chloride
(HTCC), heparin (Hep), and tannic acid (TA) fabricated under physiological
conditions with the ability to release heparin-binding proteins. Surface
plasmon resonance analysis showed that the films formed on an anchoring
HTCC/TA bilayer, with TA serving as a physical crosslinker, were more
stable during their assembly, leading to increased film thickness
and increased protein release. X-ray reflectivity measurements confirmed
intermixing of the deposited layers. Protein release also increased
when the proteins were present as an integral part of the Hep layers
rather than as individual protein layers. The 4-week release pattern
depended on the protein type; VEGF, CXCL12, and TGF-β1 exhibited
a typical high initial release, whereas FGF-2 was sustainably released
over 4 weeks. Notably, the films were nontoxic, and the released proteins
retained their bioactivity, as demonstrated by the intensive chemotaxis
of T-lymphocytes in response to the released CXCL12. Therefore, the
proposed LbL films are promising biomaterial coating candidates for
stimulating cellular responses.